A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965375



Internal ID22740310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45169736..45175833hg38UCSC Ensembl
chr20:43798377..43804474hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg386098
hg196098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17396991
Samples
Known GenesPI3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965375
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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